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"Vircell" Mycoplasma Pneumoniae Test (Non-sterile) - Taiwan Registration ec9f2e272dfb824ee162a64050a24f8c

Access comprehensive regulatory information for "Vircell" Mycoplasma Pneumoniae Test (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ec9f2e272dfb824ee162a64050a24f8c and manufactured by VIRCELL, S.L. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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ec9f2e272dfb824ee162a64050a24f8c
Registration Details
Taiwan FDA Registration: ec9f2e272dfb824ee162a64050a24f8c
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Device Details

"Vircell" Mycoplasma Pneumoniae Test (Non-sterile)
TW: "ๅ‡ก่ณฝ็ˆพ" ่‚บ็‚Ž้ปดๆผฟ่Œๆชขๆธฌ่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

ec9f2e272dfb824ee162a64050a24f8c

Ministry of Health Medical Device Import No. 017336

DHA09401733608

Company Information

Spain

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Mycoplasma Serological Reagent (C.3375)".

C Immunology and microbiology devices

C3375 Mycoplasma serum reagent

Imported from abroad

Dates and Status

Dec 23, 2016

Dec 23, 2026